Tetrapeptide Inhibitors of the Glutamate Vesicular Transporter (VGLUT)

Quinoline-2,4-dicaboxylic acids (QDCs) bearing lipophilic substituents in the 6- or 7-position were shown to be inhibitors of the glutamate vesicular transporter (VGLUT). Using the arrangement of the QDC lipophilic substituents as a template, libraries of X(1)X(2)EF and X(1)X(2)EW tetrapeptides were...

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Bibliographic Details
Main Authors:	Patel, Sarjubhai A., Nagy, Jon O., Bolstad, Erin D., Gerdes, John M., Thompson, Charles M.
Format:	Artigo
Language:	Inglês
Published:	2007
Subjects:	Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC2001293/ https://ncbi.nlm.nih.gov/pubmed/17662605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2007.07.006
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Tetrapeptide Inhibitors of the Glutamate Vesicular Transporter (VGLUT)

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